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Post-Market-Surveillance - EndoWave [EN]


Post-market surveillance is a legally anchored, proactive and systematic process to derive necessary corrective and preventive measures of information about medical devices that have already been placed on the market.

Our goal is:
  • Uncover risks associated with the use of the product,
  • ensure the performance of the products,
  • Identify product defects and security issues,
  • Assess the benefits and risks
  • initiate necessary measures.
Only with systematic monitoring, even after they have been placed on the market, we can guarantee that our products offer the desired benefit and make sure that there is no uncontrolled risk for patients, users or third parties.

Thank you for taking the time to fill out this questionnaire. It will not take more than 5 minutes to fill out the form.

Please note the following when answering the questions:
  • Not all questions need to be answered. However, if you can give us valuable advice on a particular topic, it will help us if this is described in as much detail as possible.
  • The information you give us and the data from the completed questionnaires are sent directly to our European QM department, where they are summarized in the form of anonymized statistics before they are globally evaluated. They can then no longer be assigned to individuals.
Thanks for your support!

Your MORITA team